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结核分枝杆菌45千道尔顿糖蛋白上糖基化位点的证据。

Evidence for glycosylation sites on the 45-kilodalton glycoprotein of Mycobacterium tuberculosis.

作者信息

Dobos K M, Swiderek K, Khoo K H, Brennan P J, Belisle J T

机构信息

Department of Microbiology, Colorado State University, Fort Collins 80523, USA.

出版信息

Infect Immun. 1995 Aug;63(8):2846-53. doi: 10.1128/iai.63.8.2846-2853.1995.

Abstract

The occurrence of glycosylated proteins in Mycobacterium tuberculosis has been widely reported. However, unequivocal proof for the presence of true glycosylated amino acids within these proteins has not been demonstrated, and such evidence is essential because of the predominance of soluble lipoglycans and glycolipids in all mycobacterial extracts. We have confirmed the presence of several putative glycoproteins in subcellular fractions of M. tuberculosis by reaction with the lectin concanavalin A. One such product, with a molecular mass of 45 kDa, was purified from the culture filtrate. Compositional analysis demonstrated that the protein was rich in proline and that mannose, galactose, glucose, and arabinose together represented about 4% of the total mass. The 45-kDa glycoprotein was subjected to proteolytic digestion with either the Asp-N or the Glu-C endopeptidase or subtilisin, peptides were resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and glycopeptides were identified by reaction with concanavalin A. Peptides were further separated, and when they were analyzed by liquid chromatography-electrospray mass spectrometry for neutral losses of hexoses (162 mass units), four peptides were identified, indicating that these were glycosylated with hexose residues. One peptide, with an average molecular mass of 1,516 atomic mass units (AMU), exhibited a loss of two hexose units. The N-terminal sequence of the 1,516-AMU glycopeptide was determined to be DPEPAPPVP, which was identical to the sequence of the amino terminus of the mature protein, DPEPAP PVPXTA. Furthermore, analysis of the glycopeptide by secondary ion mass spectrometry demonstrated that the complete sequence of the glycopeptide was DPEPAPPVPTTA. From this, it was determined that the 10th amino acid, threonine, was O-glycosidically linked to a disaccharide composed of two hexose residues, probably mannose. This report establishes that true, O-glycosylated proteins exist in mycobacteria.

摘要

结核分枝杆菌中糖基化蛋白的存在已被广泛报道。然而,这些蛋白中真正糖基化氨基酸存在的确凿证据尚未得到证实,而由于所有分枝杆菌提取物中可溶性脂聚糖和糖脂占主导地位,这样的证据至关重要。我们通过与凝集素伴刀豆球蛋白A反应,证实了结核分枝杆菌亚细胞组分中存在几种假定的糖蛋白。从培养滤液中纯化出了一种这样的产物,分子量为45 kDa。成分分析表明该蛋白富含脯氨酸,甘露糖、半乳糖、葡萄糖和阿拉伯糖的总量约占总质量的4%。对45 kDa糖蛋白用天冬氨酸蛋白酶N或谷氨酸蛋白酶C或枯草杆菌蛋白酶进行蛋白水解消化,肽段通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分离,糖肽通过与伴刀豆球蛋白A反应鉴定。肽段进一步分离,当通过液相色谱-电喷雾质谱分析己糖(162质量单位)的中性损失时,鉴定出四个肽段,表明它们被己糖残基糖基化。一个平均分子量为1516原子质量单位(AMU)的肽段显示损失了两个己糖单位。1516 AMU糖肽的N端序列确定为DPEPAPPVP,与成熟蛋白氨基末端的序列DPEPAP PVPXTA相同。此外,通过二次离子质谱对糖肽的分析表明,糖肽的完整序列为DPEPAPPVPTTA。由此确定第10个氨基酸苏氨酸通过O-糖苷键与由两个己糖残基(可能是甘露糖)组成的二糖相连。本报告证实分枝杆菌中存在真正的O-糖基化蛋白。

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